CZ20021980A3 - Způsob výroby chloridů kyseliny o-chlormethylbenzoové - Google Patents
Způsob výroby chloridů kyseliny o-chlormethylbenzoové Download PDFInfo
- Publication number
- CZ20021980A3 CZ20021980A3 CZ20021980A CZ20021980A CZ20021980A3 CZ 20021980 A3 CZ20021980 A3 CZ 20021980A3 CZ 20021980 A CZ20021980 A CZ 20021980A CZ 20021980 A CZ20021980 A CZ 20021980A CZ 20021980 A3 CZ20021980 A3 CZ 20021980A3
- Authority
- CZ
- Czechia
- Prior art keywords
- formula
- mol
- phosgene
- process according
- catalyst
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 6
- 150000001805 chlorine compounds Chemical class 0.000 title claims 2
- YTEUDCIEJDRJTM-UHFFFAOYSA-N 2-(chloromethyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1CCl YTEUDCIEJDRJTM-UHFFFAOYSA-N 0.000 title description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims abstract description 44
- 238000006243 chemical reaction Methods 0.000 claims abstract description 24
- 239000003054 catalyst Substances 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 20
- 239000002841 Lewis acid Substances 0.000 claims abstract description 15
- 150000007517 lewis acids Chemical class 0.000 claims abstract description 15
- 150000002596 lactones Chemical class 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 claims abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- 239000000539 dimer Substances 0.000 claims abstract description 5
- 239000013638 trimer Substances 0.000 claims abstract description 5
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 4
- 150000002367 halogens Chemical class 0.000 claims abstract description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 4
- 150000002431 hydrogen Chemical class 0.000 claims abstract 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 12
- 239000004327 boric acid Substances 0.000 claims description 11
- ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 claims description 8
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 claims description 7
- -1 C 1 -C 4 -alkyl Chemical class 0.000 claims description 6
- 230000003197 catalytic effect Effects 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 2
- 150000001639 boron compounds Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 claims 2
- 229910015900 BF3 Inorganic materials 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 claims 1
- TXZFBHYDQGYOIT-UHFFFAOYSA-N 2-(chloromethyl)benzoyl chloride Chemical class ClCC1=CC=CC=C1C(Cl)=O TXZFBHYDQGYOIT-UHFFFAOYSA-N 0.000 abstract description 23
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical class C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 44
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 22
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000012043 crude product Substances 0.000 description 8
- 239000007795 chemical reaction product Substances 0.000 description 6
- 239000012320 chlorinating reagent Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 238000004508 fractional distillation Methods 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 3
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000010457 zeolite Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical class ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- HCUYBXPSSCRKRF-UHFFFAOYSA-N diphosgene Chemical compound ClC(=O)OC(Cl)(Cl)Cl HCUYBXPSSCRKRF-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical compound CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical group [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 2
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- AURDEEIHMPRBLI-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1.CC1=CC=CN=C1 AURDEEIHMPRBLI-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000005676 cyclic carbonates Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000004816 dichlorobenzenes Chemical class 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- 239000011968 lewis acid catalyst Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 125000005506 phthalide group Chemical group 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- MJCYPBSRKLJZTB-UHFFFAOYSA-N trifluoroborane;dihydrate Chemical compound O.O.FB(F)F MJCYPBSRKLJZTB-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19958601 | 1999-12-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CZ20021980A3 true CZ20021980A3 (cs) | 2002-09-11 |
Family
ID=7931493
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CZ20021980A CZ20021980A3 (cs) | 1999-12-06 | 2000-11-27 | Způsob výroby chloridů kyseliny o-chlormethylbenzoové |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6734322B1 (da) |
| EP (1) | EP2097366B1 (da) |
| JP (1) | JP4674029B2 (da) |
| KR (1) | KR100669267B1 (da) |
| CN (1) | CN1222498C (da) |
| AT (1) | ATE487689T1 (da) |
| AU (1) | AU2837201A (da) |
| BR (1) | BR0016214B1 (da) |
| CA (1) | CA2393978A1 (da) |
| CZ (1) | CZ20021980A3 (da) |
| DE (1) | DE50016027D1 (da) |
| DK (1) | DK2097366T3 (da) |
| HU (1) | HUP0203482A3 (da) |
| IL (2) | IL149502A0 (da) |
| MX (1) | MXPA02004964A (da) |
| PL (1) | PL357602A1 (da) |
| WO (1) | WO2001042183A2 (da) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100675245B1 (ko) * | 1999-12-07 | 2007-01-29 | 바스프 악티엔게젤샤프트 | Ｏ-클로로메틸벤조산 클로라이드의 제조 방법 |
| KR100870851B1 (ko) | 2004-09-17 | 2008-11-27 | 아사히 가세이 케미칼즈 가부시키가이샤 | 부생 알코올류의 공업적 분리 방법 |
| CN102160956B (zh) * | 2011-03-08 | 2013-01-02 | 江苏快达农化股份有限公司 | 光气尾气吸收、利用的方法 |
| CN110028431B (zh) | 2018-06-05 | 2021-01-08 | 沈阳化工大学 | 一种三氟乙基硫醚（亚砜）取代苯类化合物及其用途 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2655334B1 (fr) * | 1989-12-06 | 1992-02-21 | Poudres & Explosifs Ste Nale | Procede de preparation de chlorures d'acides carboxyliques chlores. |
| DE4223382A1 (de) * | 1992-07-16 | 1994-01-20 | Basf Ag | Verfahren zur Herstellung von aromatischen o-Chlormethylcarbonsäurechloriden |
| DE4412316A1 (de) * | 1994-04-11 | 1995-10-12 | Basf Ag | Verfahren zur Herstellung von o-Chlormethylbenzoesäurechloriden |
| TW337519B (en) * | 1995-10-03 | 1998-08-01 | Novartis Ag | Process for the preparation of chloromethyl carbonyl chlorides |
| WO1999016743A1 (en) * | 1997-09-30 | 1999-04-08 | Korea Research Institute Of Chemical Technology | A PROCESS FOR PREPARING o-(CARBOALKOXY) PHENYLMETHANESULFONYL CHLORIDE DERIVATIVES |
-
2000
- 2000-11-27 PL PL00357602A patent/PL357602A1/xx not_active Application Discontinuation
- 2000-11-27 DE DE50016027T patent/DE50016027D1/de not_active Expired - Lifetime
- 2000-11-27 CZ CZ20021980A patent/CZ20021980A3/cs unknown
- 2000-11-27 AT AT00993318T patent/ATE487689T1/de not_active IP Right Cessation
- 2000-11-27 AU AU28372/01A patent/AU2837201A/en not_active Abandoned
- 2000-11-27 WO PCT/EP2000/011814 patent/WO2001042183A2/de not_active Ceased
- 2000-11-27 US US10/130,826 patent/US6734322B1/en not_active Expired - Fee Related
- 2000-11-27 MX MXPA02004964A patent/MXPA02004964A/es active IP Right Grant
- 2000-11-27 KR KR1020027007182A patent/KR100669267B1/ko not_active Expired - Fee Related
- 2000-11-27 IL IL14950200A patent/IL149502A0/xx active IP Right Grant
- 2000-11-27 CA CA002393978A patent/CA2393978A1/en not_active Abandoned
- 2000-11-27 CN CNB008159874A patent/CN1222498C/zh not_active Expired - Fee Related
- 2000-11-27 HU HU0203482A patent/HUP0203482A3/hu unknown
- 2000-11-27 EP EP00993318A patent/EP2097366B1/de not_active Expired - Lifetime
- 2000-11-27 JP JP2001543485A patent/JP4674029B2/ja not_active Expired - Fee Related
- 2000-11-27 DK DK00993318.5T patent/DK2097366T3/da active
- 2000-11-27 BR BRPI0016214-0A patent/BR0016214B1/pt not_active IP Right Cessation
-
2002
- 2002-05-07 IL IL149502A patent/IL149502A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JP4674029B2 (ja) | 2011-04-20 |
| BR0016214B1 (pt) | 2010-08-24 |
| KR100669267B1 (ko) | 2007-01-18 |
| US6734322B1 (en) | 2004-05-11 |
| HUP0203482A3 (en) | 2005-11-28 |
| IL149502A (en) | 2007-03-08 |
| WO2001042183A3 (de) | 2002-05-02 |
| JP2003516374A (ja) | 2003-05-13 |
| CN1222498C (zh) | 2005-10-12 |
| DE50016027D1 (de) | 2010-12-23 |
| EP2097366B1 (de) | 2010-11-10 |
| IL149502A0 (en) | 2002-11-10 |
| HUP0203482A2 (hu) | 2003-02-28 |
| PL357602A1 (en) | 2004-07-26 |
| DK2097366T3 (da) | 2011-02-21 |
| CN1391551A (zh) | 2003-01-15 |
| MXPA02004964A (es) | 2002-09-18 |
| BR0016214A (pt) | 2002-09-17 |
| EP2097366A2 (de) | 2009-09-09 |
| CA2393978A1 (en) | 2001-06-14 |
| ATE487689T1 (de) | 2010-11-15 |
| AU2837201A (en) | 2001-06-18 |
| WO2001042183A2 (de) | 2001-06-14 |
| KR20020061630A (ko) | 2002-07-24 |
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